Evidence map›Paper›PMID 32260371›Full record

ArticleViruses2020

Novel Toscana Virus Reverse Genetics System Establishes NSs as an Antagonist of Type I Interferon Responses.

Franziska Woelfl, Psylvia Léger, Nadia Oreshkova, Felix Pahmeier, Stefan Windhaber, Jana Koch, Megan Stanifer, Gleyder Roman Sosa, Zina M Uckeley, Felix A Rey and 4 more

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 27% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 24 citations in OpenAlex.

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  13. A Look intoViruses · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 4 institutions in 3 countries.

Franziska WoelflCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Psylvia LégerCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0001-7148-7125
Nadia OreshkovaWageningen Bioveterinary Research, Department of Virology, 8221 RA Lelystad, The Netherlands.
Felix PahmeierCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-7445-2259
Stefan WindhaberCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.
Jana KochCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-3574-0805
Megan StaniferCenter for Integrative Infectious Diseases Research (CIID), Molecular Virology, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-5606-1297
Gleyder Roman SosaStructural Virology Unit, Pasteur Institute, 75015 Paris, France.
Zina M UckeleyCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0001-9770-9873
Felix A ReyStructural Virology Unit, Pasteur Institute, 75015 Paris, France.
Steeve BoulantCenter for Integrative Infectious Diseases Research (CIID), Virology, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0001-8614-4993
Jeroen KortekaasWageningen Bioveterinary Research, Department of Virology, 8221 RA Lelystad, The Netherlands.ORCID 0000-0002-0329-0176
Paul J Wichgers SchreurWageningen Bioveterinary Research, Department of Virology, 8221 RA Lelystad, The Netherlands.ORCID 0000-0001-9790-2438
Pierre-Yves LozachCellNetworks Cluster of Excellence, University Hospital Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-9966-1452
Heidelberg University · DEWageningen University & Research · NLInstitut Pasteur · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sand fly-borne Toscana virus (TOSV) is the major cause of human meningoencephalitis in the Mediterranean basin during the summer season. In this work, we have developed a T7 RNA polymerase-driven reverse genetics system to recover infectious particles of a lineage B strain of TOSV. The viral protein pattern and growth properties of the rescued virus (rTOSV) were found to be similar to those of the corresponding wild-type (wt) virus. Using this system, we genetically engineered a TOSV mutant lacking expression of the non-structural protein NSs (rTOSVɸNSs). Unlike rTOSV and the wt virus, rTOSVɸNSs was unable to (i) suppress interferon (IFN)-b messenger RNA induction; and (ii) grow efficiently in cells producing IFN-b. Together, our results highlight the importance of NSs for TOSV in evading the IFN response and provide a comprehensive toolbox to investigate the TOSV life cycle in mammalian and insect host cells, including several novel polyclonal antibodies.

Indexed as

Reverse GeneticsA549 CellsAnimalsAntibodies, ViralCell LineChlorocebus aethiopsCricetinaeDNA-Directed RNA PolymerasesGenome, ViralHumansInsectaInterferon-betaKidneyMutationSandfly fever Naples virusVero CellsAntibodies, Viralbacteriophage T7 RNA polymeraseDNA-Directed RNA PolymerasesInterferon-betaViral Nonstructural ProteinsViral ProteinsArbovirusBunyaviralesinterferonneglected diseasesPhenuiviridaePhlebovirusreverse geneticssand fly feverToscana virus

Identifiers

PMID32260371
PMCPMC7232479
OpenAlexW3014614048

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.